Pheromone syntheses: A tropical approach. Enantioselective synthesis of the (2R,6S,10S) and (2S,6S,10S) isomers of methyl 2,6,10-trimethyldodecanoate
作者:J.Tércio B. Ferreira、Paulo H.G. Zarbin
DOI:10.1016/0968-0896(96)00015-6
日期:1996.3
The enantioselective syntheses of two stereoisomers, (2R,6S,10S) and (2S,6S,10S), of methyl 2,6,10-trimethyldodecanote, out of eight possible isomers, are described , employing the stereoselective hydroboration of (-)-isopulegol (2) and (+)-neo-isopulegol (2a) as the key reaction.
描述了使用(-)的立体选择性氢硼化反应,从八种可能的异构体中,合成了2,6,10-三甲基十二烷基甲基的两个立体异构体(2R,6S,10S)和(2S,6S,10S)的对映选择性合成-异异薄荷醇(2)和(+)-新异异薄荷醇(2a)作为关键反应。